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Zantac (Ranitidine) - Adverse Event Reports - Disability - Rhabdomyolysis

 



Index of reports > Cases resulting in disability (2) > Cases with Rhabdomyolysis (2)

Below is the selection of adverse event reports related to Zantac (Ranitidine) that includes cases resulting in disability where reactions include rhabdomyolysis.

Adverse event in 87 year old female receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-03-29

Patient: 87 year old female, weighing 38.0 kg (83.6 pounds)

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Delirium, Anorexia, Depressed Level of Consciousness, Renal Failure Acute, Shock, White Blood Cell Count Increased

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Allopurinol
    Dosage: 100mg per day
    Administration route: Oral
    Start date: 2007-02-08

Zantac
    Dosage: 150mg per day
    Administration route: Oral
    Start date: 2007-02-08

Other drugs received by patient: Renivace; Artist; Amlodin; Unknown Medication



Adverse event in 87 year old female receiving Zantac (Ranitidine)

Reported by a physician from Japan on 2007-03-16

Patient: 87 year old female, weighing 38.0 kg (83.6 pounds)

Adverse reactions / side effects: Rhabdomyolysis

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Allopurinol
    Dosage: 100mg per day
    Administration route: Oral
    Start date: 2007-02-08

Zantac
    Dosage: 150mg per day
    Administration route: Oral
    Start date: 2007-02-08

Other drugs received by patient: Renivace; Artist; Amlodin; Unknown Medication

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